Intrinsic curvature in duplex DNA inhibits human Topoisomerase I

Human Topoisomerase I (hTopo I) have been known as a potential target for cancer therapy. A series of duplex DNA with different intrinsic curvatures have been designed as inhibitors to hTopo I. The activities of hTopo I on relaxing supercoiled plasmid pUC 19 are apparently diminished in the presence...

Full description

Saved in:
Bibliographic Details
Main Authors: Yang, Zhaoqi, Li, Dawei, Guo, Juanjuan, Shao, Fangwei, Li, Tianhu
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/99011
http://hdl.handle.net/10220/12779
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-99011
record_format dspace
spelling sg-ntu-dr.10356-990112020-03-07T12:34:45Z Intrinsic curvature in duplex DNA inhibits human Topoisomerase I Yang, Zhaoqi Li, Dawei Guo, Juanjuan Shao, Fangwei Li, Tianhu School of Physical and Mathematical Sciences Human Topoisomerase I (hTopo I) have been known as a potential target for cancer therapy. A series of duplex DNA with different intrinsic curvatures have been designed as inhibitors to hTopo I. The activities of hTopo I on relaxing supercoiled plasmid pUC 19 are apparently diminished in the presence of the curved DNA. More potent inhibitions and smaller IC50 are achieved by duplex DNA with higher curvatures. EMSA indicates that hTopo I can recognize the curved DNA through binding interactions. Our studies demonstrate that the activity of hTopo I can be modulated by the intrinsic curvature of linear DNA and provide a new avenue to design curved DNA as hTopo I inhibitors with high therapeutic efficiency and low toxicity. 2013-08-01T04:22:22Z 2019-12-06T20:02:18Z 2013-08-01T04:22:22Z 2019-12-06T20:02:18Z 2012 2012 Journal Article Yang, Z., Li, D., Guo, J., Shao, F.,& Li, T. (2012). Intrinsic curvature in duplex DNA inhibits Human Topoisomerase I. Bioorganic & Medicinal Chemistry Letters, 22(3), 1322-1325. 0960-894X https://hdl.handle.net/10356/99011 http://hdl.handle.net/10220/12779 10.1016/j.bmcl.2011.12.089 en Bioorganic & medicinal chemistry letters
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
description Human Topoisomerase I (hTopo I) have been known as a potential target for cancer therapy. A series of duplex DNA with different intrinsic curvatures have been designed as inhibitors to hTopo I. The activities of hTopo I on relaxing supercoiled plasmid pUC 19 are apparently diminished in the presence of the curved DNA. More potent inhibitions and smaller IC50 are achieved by duplex DNA with higher curvatures. EMSA indicates that hTopo I can recognize the curved DNA through binding interactions. Our studies demonstrate that the activity of hTopo I can be modulated by the intrinsic curvature of linear DNA and provide a new avenue to design curved DNA as hTopo I inhibitors with high therapeutic efficiency and low toxicity.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Yang, Zhaoqi
Li, Dawei
Guo, Juanjuan
Shao, Fangwei
Li, Tianhu
format Article
author Yang, Zhaoqi
Li, Dawei
Guo, Juanjuan
Shao, Fangwei
Li, Tianhu
spellingShingle Yang, Zhaoqi
Li, Dawei
Guo, Juanjuan
Shao, Fangwei
Li, Tianhu
Intrinsic curvature in duplex DNA inhibits human Topoisomerase I
author_sort Yang, Zhaoqi
title Intrinsic curvature in duplex DNA inhibits human Topoisomerase I
title_short Intrinsic curvature in duplex DNA inhibits human Topoisomerase I
title_full Intrinsic curvature in duplex DNA inhibits human Topoisomerase I
title_fullStr Intrinsic curvature in duplex DNA inhibits human Topoisomerase I
title_full_unstemmed Intrinsic curvature in duplex DNA inhibits human Topoisomerase I
title_sort intrinsic curvature in duplex dna inhibits human topoisomerase i
publishDate 2013
url https://hdl.handle.net/10356/99011
http://hdl.handle.net/10220/12779
_version_ 1681041796896915456